N-alpha-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide

95%

  • Product Code: 97560
  Alias:    Na-(2,4-dinitro-5-fluorophenyl)-L-alaninamide; N-a-(2,4-dinitro-5-fluorophenyl)-L-alaninamide; Nα- (2,4-Dinitro-5-fluorophenyl)-L-alaninamide; NAlpha-(5-fluoro-2,4-nitrophenyl)-L-alanine amide; Marfey reagent
  CAS:    95713-52-3
Molecular Weight: 272.19 g./mol Molecular Formula: C₉H₉FN₄O₅
EC Number: MDL Number: MFCD00042049
Melting Point: 229°C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: This chemical is primarily used in biochemical research as a reagent for studying enzyme activity and protein interactions. It is particularly valuable in the development of assays to measure protease activity, as it can act as a substrate or inhibitor in enzymatic reactions. Its unique structure allows it to interact selectively with specific enzymes, making it a useful tool for understanding enzyme mechanisms and kinetics. Additionally, it is employed in the synthesis of peptide derivatives and in the investigation of biochemical pathways related to amino acid metabolism. Its applications are largely confined to laboratory settings, where it contributes to advancements in enzymology and molecular biology.
Product Specification:
Test Specification
Purity 95 100%
Appearance Faint Yellow to Very Dark Yellow and Faint Orange to Dark Orange Powder
Infrared spectrum Conforms to Structure
Solubility Color Yellow to Dark Yellow
Solubility Turbidity10 mgml Acetone CLEAR
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿1,100.00
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0.250 10-20 days ฿1,950.00
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1.000 10-20 days ฿3,880.00
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5.000 10-20 days ฿16,790.00
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N-alpha-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide
This chemical is primarily used in biochemical research as a reagent for studying enzyme activity and protein interactions. It is particularly valuable in the development of assays to measure protease activity, as it can act as a substrate or inhibitor in enzymatic reactions. Its unique structure allows it to interact selectively with specific enzymes, making it a useful tool for understanding enzyme mechanisms and kinetics. Additionally, it is employed in the synthesis of peptide derivatives and in the investigation of biochemical pathways related to amino acid metabolism. Its applications are largely confined to laboratory settings, where it contributes to advancements in enzymology and molecular biology.
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